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Light-induced super-hydrophilicity and photocatalytic activity of mesoporous TiO2 thin films

Authors :
Yu, Jimmy C.
Yu, Jiaguo
Ho, Wingkei
Zhao, Jincai
Source :
Journal of Photochemistry & Photobiology A: Chemistry. May2002, Vol. 148 Issue 1-3, p331. 9p.
Publication Year :
2002

Abstract

Transparent mesoporous TiO2 (MTiO2) and TiO2 nanometer thin films were prepared on fused quartz via the modified reverse micellar and sol–gel methods. The MTiO2 and TiO2 films were characterized by X-ray photoelectron spectroscopy (XPS), atomic force microscopy (AFM), X-ray diffraction (XRD), BET surface area and UV–Vis spectrophotometry. The photoinduced super-hydrophilicity and photocatalytic activity of the films were evaluated by the water contact angle measurement and photocatalytic oxidation of acetone in air, respectively. It was found that MTiO2 thin films at 500 °C showed higher photocatalytic activity and better light-induced hydrophilicity than the TiO2 thin films. This is attributed to the following reasons: (1) MTiO2 thin films are composed of smaller monodisperse spherical particles about 15 nm diameter, and possess more mesopores between spherical particles and higher surface areas and surface roughness, (2) the monodispersity of MTiO2 particles was beneficial to the transfer and separation of photo-generated electrons and holes inside of and on the surface of TiO2 particles, and reduced the recombination of photo-generated electrons and holes. At 900 °C, the MTiO2 and TiO2 films appeared to be in the rutile phase, but showed photoinduced hydrophilicity and no photocatalytic activity. This confirmed that the mechanism of photoinduced super-hydrophilicity of the films is different from that of photocatalytic oxidation. [Copyright &y& Elsevier]

Details

Language :
English
ISSN :
10106030
Volume :
148
Issue :
1-3
Database :
Academic Search Index
Journal :
Journal of Photochemistry & Photobiology A: Chemistry
Publication Type :
Academic Journal
Accession number :
8801176
Full Text :
https://doi.org/10.1016/S1010-6030(02)00060-6